rs12351590
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12351590(A;A) |
| Make rs12351590(A;G) |
| Make rs12351590(G;G) |
| Reference | GRCh37.p10 37.5/138 |
| Chromosome | 9 |
| Position | 12108916 |
| Gene | LOC105375976 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12351590 |
| dbSNP (classic) | rs12351590 |
| ClinGen | rs12351590 |
| ebi | rs12351590 |
| HLI | rs12351590 |
| Exac | rs12351590 |
| Gnomad | rs12351590 |
| Varsome | rs12351590 |
| LitVar | rs12351590 |
| Map | rs12351590 |
| PheGenI | rs12351590 |
| Biobank | rs12351590 |
| 1000 genomes | rs12351590 |
| hgdp | rs12351590 |
| ensembl | rs12351590 |
| geneview | rs12351590 |
| scholar | rs12351590 |
| rs12351590 | |
| pharmgkb | rs12351590 |
| gwascentral | rs12351590 |
| openSNP | rs12351590 |
| 23andMe | rs12351590 |
| SNPshot | rs12351590 |
| SNPdbe | rs12351590 |
| MSV3d | rs12351590 |
| GWAS Ctlg | rs12351590 |
| GMAF | 0.2475 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23738518 ]
|
| Trait | Reading and spelling |
| Title | A genome-wide association study for reading and language abilities in two population cohorts. |
| Risk Allele | |
| P-val | 3E-6 |
| Odds Ratio | NR NR |
[PMID 20525348] Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.
